A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960175



Internal ID19216740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67386769..67393565hg38UCSC Ensembl
Outerchr9:40125300..40132100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386797
hg196801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110522
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960175
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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